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Senior Statistical Programmer I/Ii

2+ years
Not Disclosed
10 Oct. 22, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Location: Warsaw, Poland

Join AstraZeneca: Make Our Pipeline Accessible to Patients

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company dedicated to discovering, developing, and commercializing prescription medicines for some of the world’s most serious diseases. We are more than just a leading pharmaceutical company; we tackle complex challenges in a fast-paced, agile environment where innovation is encouraged.

With access to extensive capabilities and a comprehensive pipeline, you’ll be involved in numerous submissions and a diverse range of projects throughout the drug development process.

The Role

As a Statistical Programming Lead, you will provide critical support and lead all programming activities related to analysis and reporting, including Clinical Study Report (CSR) development, regulatory submissions, and the scientific utilization of data for AstraZeneca products. There are ample career progression opportunities available, including technical pathways, global project management, or line management roles.

You will work within the Programming department, which oversees the programming aspects of analysis and reporting while managing and maintaining our end-to-end standards and production tools.

Main Duties and Responsibilities

Reporting to the Director within the Statistical Programming group, your responsibilities will include:

  • Creating and validating SDTM and ADaM datasets, including dataset specifications.
  • Creating and validating safety and efficacy Tables, Listings, and Figures (TFLs).
  • Ensuring high quality in your deliverables and those of other programmers.
  • Programming independently with efficiency and attention to quality.
  • Fluently implementing good programming practices.
  • Initiating, planning, or leading team activities and tasks (a valuable asset).
  • Leading programming deliverables for clinical studies or small to medium-sized projects (an additional asset).

Requirements

To succeed in this role, you should be an experienced programmer with a strong understanding of the technical and regulatory requirements related to programming in the pharmaceutical or healthcare industry.

  • Education: Degree in Mathematics (Applied Math, Engineering, etc.), Statistics, Computer Science, Life Sciences, or equivalent.
  • Experience: At least 5 years of SAS programming experience with a solid understanding of industry standards (SDTMs, ADaMs).
  • Skills: Good project management skills are essential.

So, What’s Next?

Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it’s yours.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team that represents all backgrounds and perspectives. We believe that a diverse team enhances our work and outcomes. We welcome and encourage applications from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations regarding non-discrimination in employment and recruitment, as well as work authorization and employment eligibility verification requirements.